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CPT1A gene

carnitine palmitoyltransferase 1A

Key facts

Official symbol
CPT1A
Full name
CPT1A
Chromosome
11
Map location
11q13.3
Organism
Homo sapiens
NCBI Gene ID
1374
Also known as
CPT I, CPT1, CPT1-L, CPTI-L, L-CPT1

Function summary

The mitochondrial oxidation of long-chain fatty acids is initiated by the sequential action of carnitine palmitoyltransferase I (which is located in the outer membrane and is detergent-labile) and carnitine palmitoyltransferase II (which is located in the inner membrane and is detergent-stable), together with a carnitine-acylcarnitine translocase. CPT I is the key enzyme in the carnitine-dependent transport across the mitochondrial inner membrane and its deficiency results in a decreased rate of fatty acid beta-oxidation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

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Data source: NCBI Gene · alsesAI Gene Library